Endocrine Journal
Online ISSN : 1348-4540
Print ISSN : 0918-8959
ISSN-L : 0918-8959
Symptomatic Rathke's Cleft Cyst Coexisting with Central Diabetes Insipidus and Hypophysitis: Case Report
SEIJI HAMAKAZUNORI ARITAATSUSHI TOMINAGAMASAMI YOSHIKAWAKUNIKI EGUCHIMASAYUKI SUMIDAKOUKI INAITAKASHI NISHISAKAKAORU KURISU
Author information
JOURNAL FREE ACCESS

1999 Volume 46 Issue 1 Pages 187-192

Details
Abstract

We describe a 48-year-old female with acute onset of central diabetes insipidus followed by mild anterior pituitary dysfunction. Magnetic resonance imaging (MRI) revealed enlargement of the hypophysis-infundibulum accompanied by a cystic component. She underwent a transsphenoidal exploration of the sella turcica. Histological examination showed foreign body type xanthogranulomatous inflammation in the neurohypophysis which might have been caused by rupture of a Rathke's cleft cyst. The MRI abnormalities and anterior pituitary dysfunction improved after a short course of corticosteroid administration, but the diabetes insipidus persisted. The histological findings in this case indicated the site of RCC rupture and the direction of the progression of RCC induced neurohypophysitis and adenohypophysitis.

Content from these authors
© The Japan Endocrine Society
Previous article Next article
feedback
Top